Microsatellite instability in adenomas as a marker for hereditary nonpolyposis colorectal cancer

被引:78
|
作者
Loukola, A
Salovaara, R
Kristo, P
Moisio, AL
Kääriäinen, H
Ahtola, H
Eskelinen, M
Härkönen, N
Julkunen, R
Kangas, E
Ojala, S
Tulikoura, J
Valkamo, E
Järvinen, H
Mecklin, JP
de la Chapelle, A
Aaltonen, LA
机构
[1] Univ Helsinki, Haartman Inst, Dept Med Genet, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Haartman Inst, Dept Pathol, FIN-00014 Helsinki, Finland
[3] Family Federat Finland, Helsinki, Finland
[4] Cent Hosp, Dept Surg, Joensuu, Finland
[5] Cent Hosp Mikkeli, Dept Surg, Mikkeli, Finland
[6] Cent Hosp, Dept Surg, Lappeenranta, Finland
[7] Cent Hosp, Dept Surg, Kajaani, Finland
[8] Cent Hosp, Dept Surg, Kotka, Finland
[9] Cent Hosp, Dept Surg, Savonlinna, Finland
[10] Cent Hosp Jyvaskyla, Dept Surg, Jyvaskyla, Finland
[11] Kuopio Univ Hosp, Dept Surg, SF-70210 Kuopio, Finland
[12] Kuopio Univ Hosp, Dept Internal Med, SF-70210 Kuopio, Finland
[13] Univ Helsinki, Cent Hosp, Dept Surg 2, Helsinki, Finland
[14] Ohio State Univ, Med Res Facil, Ctr Comprehens Canc, Human Canc Genet Program, Columbus, OH 43210 USA
来源
AMERICAN JOURNAL OF PATHOLOGY | 1999年 / 155卷 / 06期
关键词
D O I
10.1016/S0002-9440(10)65503-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Hereditary nonpolyposis colorectal cancer (HNPCC) is the most common of the well-defined colorectal cancer syndromes, accounting for at least 2% of the total colorectal cancer burden and carrying a greater than 80% lifetime risk of cancer. Significant reduction in cancer morbidity and mortality can be accomplished by appropriate clinical cancer screening of HNPCC patients with mutations in mismatch repair (MMR) genes. Thus, it is desirable to identify individuals who are mutation-positive. In individuals with cancer, mutation detection can be accomplished relatively efficiently by germline mutation analysis of individuals whose cancers show microsatellite instability (MSI). This study was designed to assess the feasibility of screening colorectal adenoma patients for HNPCC in the same manner. Among 378 adenoma patients, six (1.6%) had at least one MSI adenoma. Five out of the six patients (83%) had a germline MMR gene mutation. We conclude that MSI analysis is a useful method of prescreening colorectal adenoma patients for HNPCC.
引用
收藏
页码:1849 / 1853
页数:5
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